Evidence map›Paper›PMID 41566892›Full record

Trial reportJournal of the International AIDS Society2026

A cluster randomized trial of Visitect CD4 Advanced Disease platform among outpatients with advanced HIV disease in Uganda.

Elizabeth Nalintya, Elizabeth L Schwartz, Patricia Nerima, Ann Fieberg, Sarah M Najjuka, Ruth E Ajilong, Tessa Adzemovic, Olive Namakula, Atukunda Mucunguzi, Kiiza Kandole Tadeo and 9 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the International AIDS Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Elizabeth NalintyaInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Elizabeth L SchwartzDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Patricia NerimaInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Ann FiebergDivision of Biostatistics and Health Data Science, School of Public Health, University of Minnesota, Minneapolis, Minnesota, USA.
Sarah M NajjukaInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Ruth E AjilongInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Tessa AdzemovicInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Olive NamakulaInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Atukunda MucunguziInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Kiiza Kandole TadeoInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Mark OilorInfectious Diseases Institute, Makerere University, Kampala, Uganda.
Preethiya SekarUniversity of Minnesota Medical School, Minneapolis, Minnesota, USA.
Alice LehmanDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Bruce LarsonBoston University School of Public Health, Boston, Massachusetts, USA.
Biyue DaiDivision of Biostatistics and Health Data Science, School of Public Health, University of Minnesota, Minneapolis, Minnesota, USA.
David B MeyaInfectious Diseases Institute, Makerere University, Kampala, Uganda.
David R BoulwareDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Radha RajasinghamDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
ENCORE team

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UM1TR004405 · NCATS · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar, Damien A Fair · 2023 to 2026
$30.8M
NPGH LEADERs YR12: OBSSR (Greenberg, Ngwafong Mukere) & NIBIB (Lee)D43TW009345 · FIC · UNIVERSITY OF WASHINGTON · PI Dibyadyuti Datta, Chandy C. John · 2017 to 2026
$15.2M
Medical Scientist Training ProgramT32GM152284 · NIGMS · VANDERBILT UNIVERSITY · PI Christopher S. Williams · 2024 to 2026
$4.8M
An Enhanced Package of Care to Reduce Mortality in Persons with Advanced HIV DiseaseR01AI162181 · NIAID · UNIVERSITY OF MINNESOTA · PI RAJASINGHAM, RADHA · 2021 to 2025
$3.2M
FIC NIH HHS D43TW009345National Institute of Allergy and Infectious Diseases K23AI138851National Institute of Allergy and Infectious Diseases K24AI184270National Institute of Allergy and Infectious Diseases T32AI055433NCATS NIH HHS UM1TR004405NIAID NIH HHS R01 AI162181NIGMS NIH HHS T32 GM152284NIH HHS
6 · The paper itself

Abstract

introductionDespite significant progress in HIV care globally, a persistent 30-40% of people present with advanced HIV disease with ≤200 CD4 cells/µl. The Visitect CD4 Advanced Disease platform is a point-of-care CD4 test being implemented in resource-limited settings. We sought to assess clinical outcomes of survival and retention-in-care among people with advanced HIV disease based on CD4 testing modality.

methodsWe performed a cluster randomized clinical trial to evaluate the Visitect CD4 compared with onsite standard laboratory-based CD4 testing. The trial was conducted at 16 outpatient HIV clinics in Uganda. Those identified with CD4≤200 cells/µl received a standardized package of care for advanced HIV disease. The primary outcome was 24-week survival with retention-in-care. A costing analysis was performed. Randomization by CD4 methodology was stopped on 18 June, 2024, as the Visitect CD4 Advanced Disease platform was being implemented widely in Uganda, and randomization to non-Visitect CD4 platforms was unethical if no alternative CD4 strategies were available in a timely manner. We conducted a micro-costing analysis to estimate the resources used for each trial participant over the 6-month study period.

resultsBetween 5 May 2022 and 18 February 2025, 1724 participants were enrolled; 927 participants received Visitect CD4 testing (eight clusters), and 797 received standard CD4 testing (eight clusters). The composite endpoint of death or lost to follow-up occurred in 7.0% (63/901) who received Visitect CD4 testing and 7.2% (57/788) who received standard CD4 testing (hazard ratio, 0.98; 95% CI, 0.69, 1.40). The estimated risk difference between arms was 0.01% (95% CI, -2.5, 2.5). Median time to antiretroviral therapy initiation was 0 days with Visitect testing versus 7 days with standard CD4 testing (adjusted hazard ratio, 1.23; 95% CI, 1.05, 1.45). Mean cost of 6-month care was US$115 for Visitect CD4 testing versus US$131 for standard-of-care CD4 testing.

conclusionsImplementation of Visitect CD4 testing demonstrated more rapid initiation of HIV therapy with equivalent 24-week survival and retention-in-care compared with other point-of-care CD4 strategies at equivalent cost. Despite its poor specificity, the Visitect CD4 platform remains a cost-neutral option compared to standard CD4 modalities. ARTICLE SUMMARY LINE: In this cluster randomized trial, we identified that participants with advanced HIV disease who were randomized to receive the Visitect CD4 Advanced Disease platform had equivalent 24-week survival with retention-in-care compared with standard CD4 testing strategies.

Indexed as

HIV InfectionsAdultAnti-HIV AgentsCD4 Lymphocyte CountFemaleHumansMaleMiddle AgedOutpatientsPoint-of-Care SystemsPoint-of-Care TestingRetention in CareUgandaAnti-HIV Agentsadvanced HIV diseaseCD4 countopportunistic infectionspoint‐of‐careVisitect

Identifiers

PMID41566892
PMCPMC12824445

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.